Canonical Allele Identifier: CA1219517258

Gene: INAVA

Linked Data

• dbSNP Id: rs1653792978

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200912414T>C , CM000663.2:g.200912414T>C	GRCh38
NC_000001.10:g.200881542T>C , CM000663.1:g.200881542T>C	GRCh37
NC_000001.9:g.199148165T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413687.3:c.1644+277T>C MANE Select	ENSP00000392105.2:n.1644+277T>C
ENST00000367342.8:c.1899+277T>C	ENSP00000356311.4:n.1899+277T>C
ENST00000413687.2:c.1644+277T>C	ENSP00000392105.2:n.1644+277T>C
ENST00000465162.1:n.179+277T>C
NM_001142569.2:c.1644+277T>C	NP_001136041.1:n.1644+277T>C
NM_018265.3:c.1941+277T>C	NP_060735.3:n.1941+277T>C
XM_011509754.1:c.1644+277T>C	XP_011508056.1:n.1644+277T>C
XM_011509755.1:c.1644+277T>C	XP_011508057.1:n.1644+277T>C
XM_011509754.2:c.1644+277T>C	XP_011508056.1:n.1644+277T>C
NM_001142569.3:c.1644+277T>C MANE Select	NP_001136041.1:n.1644+277T>C
NM_001367289.1:c.1584+337T>C	NP_001354218.1:n.1584+337T>C
NM_001367290.1:c.1107+277T>C	NP_001354219.1:n.1107+277T>C
NM_018265.4:c.1899+277T>C	NP_060735.4:n.1899+277T>C